-
1
-
-
0033975061
-
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
-
Haider N.B., Jacobson S.G., Cideciyan A.V., et al. Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. Nat Genet 24 (2000) 127-131
-
(2000)
Nat Genet
, vol.24
, pp. 127-131
-
-
Haider, N.B.1
Jacobson, S.G.2
Cideciyan, A.V.3
-
2
-
-
0141722455
-
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration
-
Sharon D., Sandberg M.A., Caruso R.C., et al. Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration. Arch Ophthalmol 121 (2003) 1316-1323
-
(2003)
Arch Ophthalmol
, vol.121
, pp. 1316-1323
-
-
Sharon, D.1
Sandberg, M.A.2
Caruso, R.C.3
-
4
-
-
0028927183
-
Enhanced S cone syndrome: evidence for an abnormally large number of S cones
-
Hood D.C., Cideciyan A.V., Roman A.J., and Jacobson S.G. Enhanced S cone syndrome: evidence for an abnormally large number of S cones. Vision Res 35 (1995) 1473-1481
-
(1995)
Vision Res
, vol.35
, pp. 1473-1481
-
-
Hood, D.C.1
Cideciyan, A.V.2
Roman, A.J.3
Jacobson, S.G.4
-
6
-
-
0025817471
-
Relatively enhanced S cone function in the Goldmann-Favre syndrome
-
Jacobson S.G., Román A.J., Román M.I., et al. Relatively enhanced S cone function in the Goldmann-Favre syndrome. Am J Ophthalmol 111 (1991) 446-453
-
(1991)
Am J Ophthalmol
, vol.111
, pp. 446-453
-
-
Jacobson, S.G.1
Román, A.J.2
Román, M.I.3
-
7
-
-
0025333641
-
Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity
-
Marmor M.F., Jacobson S.G., Foerster M.H., et al. Diagnostic clinical findings of a new syndrome with night blindness, maculopathy, and enhanced S cone sensitivity. Am J Ophthalmol 110 (1990) 124-134
-
(1990)
Am J Ophthalmol
, vol.110
, pp. 124-134
-
-
Marmor, M.F.1
Jacobson, S.G.2
Foerster, M.H.3
-
8
-
-
12944293118
-
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
-
Akhmedov N.B., Piriev N.I., Chang B., et al. A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse. Proc Natl Acad Sci U S A 97 (2000) 5551-5556
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 5551-5556
-
-
Akhmedov, N.B.1
Piriev, N.I.2
Chang, B.3
-
9
-
-
18244385003
-
The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration
-
Milam A.H., Rose L., Cideciyan A.V., et al. The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration. Proc Natl Acad Sci U S A 99 (2002) 473-478
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 473-478
-
-
Milam, A.H.1
Rose, L.2
Cideciyan, A.V.3
-
10
-
-
0035421442
-
Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice
-
Haider N.B., Naggert J.K., and Nishina P.M. Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice. Hum Mol Genet 10 (2001) 1619-1626
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1619-1626
-
-
Haider, N.B.1
Naggert, J.K.2
Nishina, P.M.3
-
11
-
-
4544267698
-
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
-
Jacobson S.G., Sumaroka A., Aleman T.S., et al. Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. Hum Mol Genet 13 (2004) 1893-1902
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1893-1902
-
-
Jacobson, S.G.1
Sumaroka, A.2
Aleman, T.S.3
-
12
-
-
2442539067
-
Distribution of short-wavelength-sensitive cones in human fetal and postnatal retina: early development of spatial order and density profiles
-
Cornish E.A., Hendrickson A.E., and Provis J.M. Distribution of short-wavelength-sensitive cones in human fetal and postnatal retina: early development of spatial order and density profiles. Vision Res 44 (2004) 2019-2026
-
(2004)
Vision Res
, vol.44
, pp. 2019-2026
-
-
Cornish, E.A.1
Hendrickson, A.E.2
Provis, J.M.3
-
13
-
-
10644231018
-
Fixation pattern and macular sensitivity in eyes with subfoveal choroidal neovascularization secondary to age-related macular degeneration. A microperimetry study
-
Midena E., Radin P.P., Pilotto E., et al. Fixation pattern and macular sensitivity in eyes with subfoveal choroidal neovascularization secondary to age-related macular degeneration. A microperimetry study. Semin Ophthalmol 19 (2004) 55-61
-
(2004)
Semin Ophthalmol
, vol.19
, pp. 55-61
-
-
Midena, E.1
Radin, P.P.2
Pilotto, E.3
-
14
-
-
65449184666
-
Technical insights in the interpretation of automatic microperimetry
-
Midena E. (Ed), SLACK Inc., Thorofare, NJ
-
Convento E., and Barbaro G. Technical insights in the interpretation of automatic microperimetry. In: Midena E. (Ed). Perimetry and the Fundus: An Introduction to Microperimetry (2007), SLACK Inc., Thorofare, NJ 229-237
-
(2007)
Perimetry and the Fundus: An Introduction to Microperimetry
, pp. 229-237
-
-
Convento, E.1
Barbaro, G.2
-
15
-
-
0032990052
-
Measuring geographic atrophy in advanced age-related macular degeneration
-
Sunness J.S., Bressler N.M., Tian Y., et al. Measuring geographic atrophy in advanced age-related macular degeneration. Invest Ophthalmol Vis Sci 40 (1999) 1761-1769
-
(1999)
Invest Ophthalmol Vis Sci
, vol.40
, pp. 1761-1769
-
-
Sunness, J.S.1
Bressler, N.M.2
Tian, Y.3
-
16
-
-
0031952382
-
Topography of diabetic macular edema with optical coherence tomography
-
Hee M.R., Puliafito C.A., Duker J.S., et al. Topography of diabetic macular edema with optical coherence tomography. Ophthalmology 105 (1998) 360-370
-
(1998)
Ophthalmology
, vol.105
, pp. 360-370
-
-
Hee, M.R.1
Puliafito, C.A.2
Duker, J.S.3
-
17
-
-
33746679982
-
Diabetic macular edema: correlation between microperimetry and optical coherence tomography findings
-
Vujosevic S., Midena E., Pilotto E., et al. Diabetic macular edema: correlation between microperimetry and optical coherence tomography findings. Invest Ophthalmol Vis Sci 47 (2006) 3044-3051
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 3044-3051
-
-
Vujosevic, S.1
Midena, E.2
Pilotto, E.3
-
18
-
-
56149108242
-
Comparison of macular thickness measurements between time domain and spectral domain optical coherence tomography
-
Leung C.K., Cheung C.Y., Weinreb R.N., et al. Comparison of macular thickness measurements between time domain and spectral domain optical coherence tomography. Invest Ophthalmol Vis Sci 49 (2008) 4893-4897
-
(2008)
Invest Ophthalmol Vis Sci
, vol.49
, pp. 4893-4897
-
-
Leung, C.K.1
Cheung, C.Y.2
Weinreb, R.N.3
-
19
-
-
38949204932
-
Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance
-
Vaclavik V., Chakarova C., Bhattacharya S.S., et al. Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance. Br J Ophthalmol 92 (2008) 299-300
-
(2008)
Br J Ophthalmol
, vol.92
, pp. 299-300
-
-
Vaclavik, V.1
Chakarova, C.2
Bhattacharya, S.S.3
-
20
-
-
0024378477
-
Cell loss in the aging retina. Relationship to lipofuscin accumulation and macular degeneration
-
Dorey C.K., Wu G., Ebenstein D., et al. Cell loss in the aging retina. Relationship to lipofuscin accumulation and macular degeneration. Invest Ophthalmol Vis Sci 30 (1989) 1691-1699
-
(1989)
Invest Ophthalmol Vis Sci
, vol.30
, pp. 1691-1699
-
-
Dorey, C.K.1
Wu, G.2
Ebenstein, D.3
-
21
-
-
0344830731
-
Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope
-
von Rückmann A., Fitzke F.W., and Bird A.C. Fundus autofluorescence in age-related macular disease imaged with a laser scanning ophthalmoscope. Invest Ophthalmol Vis Sci 38 (1997) 478-486
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 478-486
-
-
von Rückmann, A.1
Fitzke, F.W.2
Bird, A.C.3
-
22
-
-
33144472133
-
A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome
-
Corbo J.C., and Cepko C.L. A hybrid photoreceptor expressing both rod and cone genes in a mouse model of enhanced S-cone syndrome. PLoS Genet 1 (2005) e11
-
(2005)
PLoS Genet
, vol.1
-
-
Corbo, J.C.1
Cepko, C.L.2
-
23
-
-
0036964799
-
Elevated macular retinoschisis associated with Goldmann-Favre syndrome successfully treated with grid laser photocoagulation
-
Khairallah M., Ladjimi A., Ben Yahia S., et al. Elevated macular retinoschisis associated with Goldmann-Favre syndrome successfully treated with grid laser photocoagulation. Retina 22 (2002) 234-237
-
(2002)
Retina
, vol.22
, pp. 234-237
-
-
Khairallah, M.1
Ladjimi, A.2
Ben Yahia, S.3
-
24
-
-
58249121842
-
Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide
-
Iannaccone A., Fung K.H., Eyestone M.E., et al. Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide. Am J Ophthalmol 147 (2009) 307-312
-
(2009)
Am J Ophthalmol
, vol.147
, pp. 307-312
-
-
Iannaccone, A.1
Fung, K.H.2
Eyestone, M.E.3
-
25
-
-
77952891588
-
Dorzolamide use in the management of macular cysts in a patient with enhanced S-cone syndrome
-
Hajali M., and Fishman G.A. Dorzolamide use in the management of macular cysts in a patient with enhanced S-cone syndrome. Retin Cases Brief Rep 3 (2009) 121-124
-
(2009)
Retin Cases Brief Rep
, vol.3
, pp. 121-124
-
-
Hajali, M.1
Fishman, G.A.2
-
26
-
-
0032588081
-
Müller cell cone, an overlooked part of the anatomy of the fovea centralis: hypotheses concerning its role in the pathogenesis of macular hole and foveomacular retinoschisis
-
Gass J.D. Müller cell cone, an overlooked part of the anatomy of the fovea centralis: hypotheses concerning its role in the pathogenesis of macular hole and foveomacular retinoschisis. Arch Ophthalmol 117 (1999) 821-823
-
(1999)
Arch Ophthalmol
, vol.117
, pp. 821-823
-
-
Gass, J.D.1
-
27
-
-
56649114571
-
CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene
-
Langmann T., Lai C.C., Weigelt K., et al. CRX controls retinal expression of the X-linked juvenile retinoschisis (RS1) gene. Nucleic Acids Res 36 (2008) 6523-6534
-
(2008)
Nucleic Acids Res
, vol.36
, pp. 6523-6534
-
-
Langmann, T.1
Lai, C.C.2
Weigelt, K.3
-
28
-
-
0033592987
-
Retina-specific nuclear receptor: a potential regulator of cellular retinaldehyde-binding protein expressed in retinal pigment epithelium and Müller glial cells
-
Chen F., Figueroa D.J., Marmorstein A.D., et al. Retina-specific nuclear receptor: a potential regulator of cellular retinaldehyde-binding protein expressed in retinal pigment epithelium and Müller glial cells. Proc Natl Acad Sci U S A 96 (1999) 15149-15154
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 15149-15154
-
-
Chen, F.1
Figueroa, D.J.2
Marmorstein, A.D.3
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